MX2007006733A - Composition. - Google Patents
Composition.Info
- Publication number
- MX2007006733A MX2007006733A MX2007006733A MX2007006733A MX2007006733A MX 2007006733 A MX2007006733 A MX 2007006733A MX 2007006733 A MX2007006733 A MX 2007006733A MX 2007006733 A MX2007006733 A MX 2007006733A MX 2007006733 A MX2007006733 A MX 2007006733A
- Authority
- MX
- Mexico
- Prior art keywords
- polymer
- composition
- added
- amount
- paper
- Prior art date
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 134
- 229920000642 polymer Polymers 0.000 claims abstract description 77
- 239000000725 suspension Substances 0.000 claims abstract description 66
- 238000000034 method Methods 0.000 claims abstract description 39
- 239000002736 nonionic surfactant Substances 0.000 claims abstract description 33
- 230000008569 process Effects 0.000 claims abstract description 27
- 125000000129 anionic group Chemical group 0.000 claims abstract description 20
- 238000004519 manufacturing process Methods 0.000 claims abstract description 19
- 125000002091 cationic group Chemical group 0.000 claims abstract description 18
- 239000003945 anionic surfactant Substances 0.000 claims abstract description 17
- 150000001449 anionic compounds Chemical class 0.000 claims abstract description 13
- 239000011859 microparticle Substances 0.000 claims abstract description 9
- 239000000835 fiber Substances 0.000 claims description 54
- 239000003921 oil Substances 0.000 claims description 37
- 235000019198 oils Nutrition 0.000 claims description 37
- 239000004094 surface-active agent Substances 0.000 claims description 29
- 150000002191 fatty alcohols Chemical class 0.000 claims description 13
- 125000003118 aryl group Chemical group 0.000 claims description 10
- 235000014113 dietary fatty acids Nutrition 0.000 claims description 10
- 239000000194 fatty acid Substances 0.000 claims description 10
- 229930195729 fatty acid Natural products 0.000 claims description 10
- 150000004665 fatty acids Chemical class 0.000 claims description 10
- 125000000217 alkyl group Chemical group 0.000 claims description 9
- 235000019197 fats Nutrition 0.000 claims description 9
- 125000001453 quaternary ammonium group Chemical group 0.000 claims description 9
- 239000003240 coconut oil Substances 0.000 claims description 8
- 235000019864 coconut oil Nutrition 0.000 claims description 8
- 229920006317 cationic polymer Polymers 0.000 claims description 5
- 229920003043 Cellulose fiber Polymers 0.000 claims description 3
- 229910019142 PO4 Inorganic materials 0.000 claims description 3
- ABLZXFCXXLZCGV-UHFFFAOYSA-N Phosphorous acid Chemical class OP(O)=O ABLZXFCXXLZCGV-UHFFFAOYSA-N 0.000 claims description 3
- 235000021317 phosphate Nutrition 0.000 claims description 3
- 150000003013 phosphoric acid derivatives Chemical class 0.000 claims description 3
- 150000003014 phosphoric acid esters Chemical class 0.000 claims description 3
- 150000003871 sulfonates Chemical class 0.000 claims description 3
- 150000003467 sulfuric acid derivatives Chemical class 0.000 claims description 3
- 235000015112 vegetable and seed oil Nutrition 0.000 claims description 2
- 239000008158 vegetable oil Substances 0.000 claims description 2
- 230000002708 enhancing effect Effects 0.000 abstract 1
- 239000000123 paper Substances 0.000 description 96
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 18
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 16
- 239000000839 emulsion Substances 0.000 description 15
- 238000012360 testing method Methods 0.000 description 15
- 239000000126 substance Substances 0.000 description 14
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 12
- 239000000243 solution Substances 0.000 description 11
- 238000002156 mixing Methods 0.000 description 10
- 229920002472 Starch Polymers 0.000 description 9
- 239000007864 aqueous solution Substances 0.000 description 9
- 239000004519 grease Substances 0.000 description 9
- 235000019698 starch Nutrition 0.000 description 9
- 239000001993 wax Substances 0.000 description 9
- 239000002245 particle Substances 0.000 description 8
- 238000007792 addition Methods 0.000 description 7
- 150000001875 compounds Chemical class 0.000 description 7
- 239000006210 lotion Substances 0.000 description 7
- 238000009736 wetting Methods 0.000 description 7
- 229920001131 Pulp (paper) Polymers 0.000 description 6
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 6
- 125000004432 carbon atom Chemical group C* 0.000 description 6
- 229920002678 cellulose Polymers 0.000 description 6
- 239000001913 cellulose Substances 0.000 description 6
- 239000003795 chemical substances by application Substances 0.000 description 6
- 239000008119 colloidal silica Substances 0.000 description 6
- -1 polysiloxane Polymers 0.000 description 6
- 239000008107 starch Substances 0.000 description 6
- 229910021653 sulphate ion Inorganic materials 0.000 description 6
- 235000008331 Pinus X rigitaeda Nutrition 0.000 description 5
- 235000011613 Pinus brutia Nutrition 0.000 description 5
- 241000018646 Pinus brutia Species 0.000 description 5
- 239000002253 acid Substances 0.000 description 5
- 238000006243 chemical reaction Methods 0.000 description 5
- 230000001143 conditioned effect Effects 0.000 description 5
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 4
- 230000015572 biosynthetic process Effects 0.000 description 4
- GQOKIYDTHHZSCJ-UHFFFAOYSA-M dimethyl-bis(prop-2-enyl)azanium;chloride Chemical compound [Cl-].C=CC[N+](C)(C)CC=C GQOKIYDTHHZSCJ-UHFFFAOYSA-M 0.000 description 4
- 239000000377 silicon dioxide Substances 0.000 description 4
- 239000004359 castor oil Substances 0.000 description 3
- 235000019438 castor oil Nutrition 0.000 description 3
- 238000001035 drying Methods 0.000 description 3
- 239000003974 emollient agent Substances 0.000 description 3
- ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 description 3
- 230000014759 maintenance of location Effects 0.000 description 3
- 229920000768 polyamine Polymers 0.000 description 3
- 238000003756 stirring Methods 0.000 description 3
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 description 2
- VVJKKWFAADXIJK-UHFFFAOYSA-N Allylamine Chemical compound NCC=C VVJKKWFAADXIJK-UHFFFAOYSA-N 0.000 description 2
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 2
- 244000303965 Cyamopsis psoralioides Species 0.000 description 2
- 229920002873 Polyethylenimine Polymers 0.000 description 2
- 240000008042 Zea mays Species 0.000 description 2
- 235000002017 Zea mays subsp mays Nutrition 0.000 description 2
- 230000002745 absorbent Effects 0.000 description 2
- 239000002250 absorbent Substances 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 229910052782 aluminium Inorganic materials 0.000 description 2
- 229920006318 anionic polymer Polymers 0.000 description 2
- 230000009172 bursting Effects 0.000 description 2
- 229920001577 copolymer Polymers 0.000 description 2
- 230000007423 decrease Effects 0.000 description 2
- 230000001804 emulsifying effect Effects 0.000 description 2
- 229910021485 fumed silica Inorganic materials 0.000 description 2
- 230000006870 function Effects 0.000 description 2
- 239000000976 ink Substances 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 238000006116 polymerization reaction Methods 0.000 description 2
- 229920001282 polysaccharide Polymers 0.000 description 2
- 239000005017 polysaccharide Substances 0.000 description 2
- 229920001296 polysiloxane Polymers 0.000 description 2
- 238000003825 pressing Methods 0.000 description 2
- 230000009467 reduction Effects 0.000 description 2
- 230000035807 sensation Effects 0.000 description 2
- 229910021487 silica fume Inorganic materials 0.000 description 2
- 230000003068 static effect Effects 0.000 description 2
- 238000012546 transfer Methods 0.000 description 2
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 1
- 244000144927 Aloe barbadensis Species 0.000 description 1
- 235000002961 Aloe barbadensis Nutrition 0.000 description 1
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 description 1
- 229920002101 Chitin Polymers 0.000 description 1
- 229920001661 Chitosan Polymers 0.000 description 1
- 244000060011 Cocos nucifera Species 0.000 description 1
- 235000013162 Cocos nucifera Nutrition 0.000 description 1
- 229920001353 Dextrin Polymers 0.000 description 1
- 239000004375 Dextrin Substances 0.000 description 1
- BRLQWZUYTZBJKN-UHFFFAOYSA-N Epichlorohydrin Chemical compound ClCC1CO1 BRLQWZUYTZBJKN-UHFFFAOYSA-N 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- 229920001503 Glucan Polymers 0.000 description 1
- 240000005979 Hordeum vulgare Species 0.000 description 1
- 235000007340 Hordeum vulgare Nutrition 0.000 description 1
- 240000003183 Manihot esculenta Species 0.000 description 1
- 235000016735 Manihot esculenta subsp esculenta Nutrition 0.000 description 1
- 229920000057 Mannan Polymers 0.000 description 1
- 240000007594 Oryza sativa Species 0.000 description 1
- 235000007164 Oryza sativa Nutrition 0.000 description 1
- 235000019482 Palm oil Nutrition 0.000 description 1
- 235000019484 Rapeseed oil Nutrition 0.000 description 1
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 1
- 239000004115 Sodium Silicate Substances 0.000 description 1
- 239000004902 Softening Agent Substances 0.000 description 1
- 244000061456 Solanum tuberosum Species 0.000 description 1
- 235000002595 Solanum tuberosum Nutrition 0.000 description 1
- 235000019486 Sunflower oil Nutrition 0.000 description 1
- 235000021307 Triticum Nutrition 0.000 description 1
- 244000098338 Triticum aestivum Species 0.000 description 1
- 235000005824 Zea mays ssp. parviglumis Nutrition 0.000 description 1
- 235000016383 Zea mays subsp huehuetenangensis Nutrition 0.000 description 1
- NJSSICCENMLTKO-HRCBOCMUSA-N [(1r,2s,4r,5r)-3-hydroxy-4-(4-methylphenyl)sulfonyloxy-6,8-dioxabicyclo[3.2.1]octan-2-yl] 4-methylbenzenesulfonate Chemical compound C1=CC(C)=CC=C1S(=O)(=O)O[C@H]1C(O)[C@@H](OS(=O)(=O)C=2C=CC(C)=CC=2)[C@@H]2OC[C@H]1O2 NJSSICCENMLTKO-HRCBOCMUSA-N 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 150000003926 acrylamides Chemical class 0.000 description 1
- 150000001252 acrylic acid derivatives Chemical class 0.000 description 1
- 235000011399 aloe vera Nutrition 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 238000013459 approach Methods 0.000 description 1
- CADWTSSKOVRVJC-UHFFFAOYSA-N benzyl(dimethyl)azanium;chloride Chemical compound [Cl-].C[NH+](C)CC1=CC=CC=C1 CADWTSSKOVRVJC-UHFFFAOYSA-N 0.000 description 1
- 229910052796 boron Inorganic materials 0.000 description 1
- 239000012267 brine Substances 0.000 description 1
- 238000003490 calendering Methods 0.000 description 1
- 239000001569 carbon dioxide Substances 0.000 description 1
- 229910002092 carbon dioxide Inorganic materials 0.000 description 1
- 238000007156 chain growth polymerization reaction Methods 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 235000005822 corn Nutrition 0.000 description 1
- 239000002537 cosmetic Substances 0.000 description 1
- 239000000490 cosmetic additive Substances 0.000 description 1
- GVJHHUAWPYXKBD-UHFFFAOYSA-N d-alpha-tocopherol Natural products OC1=C(C)C(C)=C2OC(CCCC(C)CCCC(C)CCCC(C)C)(C)CCC2=C1C GVJHHUAWPYXKBD-UHFFFAOYSA-N 0.000 description 1
- 230000006735 deficit Effects 0.000 description 1
- 239000002761 deinking Substances 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 235000019425 dextrin Nutrition 0.000 description 1
- IQDGSYLLQPDQDV-UHFFFAOYSA-N dimethylazanium;chloride Chemical class Cl.CNC IQDGSYLLQPDQDV-UHFFFAOYSA-N 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 239000003995 emulsifying agent Substances 0.000 description 1
- 238000005265 energy consumption Methods 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- UYMKPFRHYYNDTL-UHFFFAOYSA-N ethenamine Chemical compound NC=C UYMKPFRHYYNDTL-UHFFFAOYSA-N 0.000 description 1
- 230000001815 facial effect Effects 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 239000000499 gel Substances 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 239000003292 glue Substances 0.000 description 1
- 150000004676 glycans Chemical class 0.000 description 1
- 239000008169 grapeseed oil Substances 0.000 description 1
- 230000002209 hydrophobic effect Effects 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 229920000831 ionic polymer Polymers 0.000 description 1
- 239000002655 kraft paper Substances 0.000 description 1
- 235000009973 maize Nutrition 0.000 description 1
- LUEWUZLMQUOBSB-GFVSVBBRSA-N mannan Chemical class O[C@H]1[C@@H](O)[C@H](O)[C@@H](CO)O[C@H]1O[C@@H]1[C@@H](CO)O[C@@H](O[C@@H]2[C@H](O[C@@H](O[C@H]3[C@H](O[C@@H](O)[C@@H](O)[C@H]3O)CO)[C@@H](O)[C@H]2O)CO)[C@H](O)[C@H]1O LUEWUZLMQUOBSB-GFVSVBBRSA-N 0.000 description 1
- WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical compound O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 description 1
- 239000002480 mineral oil Substances 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- PSZYNBSKGUBXEH-UHFFFAOYSA-M naphthalene-1-sulfonate Chemical compound C1=CC=C2C(S(=O)(=O)[O-])=CC=CC2=C1 PSZYNBSKGUBXEH-UHFFFAOYSA-M 0.000 description 1
- 229920005615 natural polymer Polymers 0.000 description 1
- 239000004006 olive oil Substances 0.000 description 1
- 235000008390 olive oil Nutrition 0.000 description 1
- 229920000620 organic polymer Polymers 0.000 description 1
- 239000002540 palm oil Substances 0.000 description 1
- 229920001277 pectin Polymers 0.000 description 1
- 239000001814 pectin Substances 0.000 description 1
- 235000010987 pectin Nutrition 0.000 description 1
- 229920000371 poly(diallyldimethylammonium chloride) polymer Polymers 0.000 description 1
- 229920001467 poly(styrenesulfonates) Polymers 0.000 description 1
- 239000011970 polystyrene sulfonate Substances 0.000 description 1
- 229920002635 polyurethane Polymers 0.000 description 1
- 239000004814 polyurethane Substances 0.000 description 1
- 239000003755 preservative agent Substances 0.000 description 1
- 108090000623 proteins and genes Proteins 0.000 description 1
- ROSDSFDQCJNGOL-UHFFFAOYSA-N protonated dimethyl amine Natural products CNC ROSDSFDQCJNGOL-UHFFFAOYSA-N 0.000 description 1
- 235000009566 rice Nutrition 0.000 description 1
- RMAQACBXLXPBSY-UHFFFAOYSA-N silicic acid Chemical compound O[Si](O)(O)O RMAQACBXLXPBSY-UHFFFAOYSA-N 0.000 description 1
- 239000010703 silicon Substances 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- 229910021647 smectite Inorganic materials 0.000 description 1
- NTHWMYGWWRZVTN-UHFFFAOYSA-N sodium silicate Chemical compound [Na+].[Na+].[O-][Si]([O-])=O NTHWMYGWWRZVTN-UHFFFAOYSA-N 0.000 description 1
- 229910052911 sodium silicate Inorganic materials 0.000 description 1
- HPALAKNZSZLMCH-UHFFFAOYSA-M sodium;chloride;hydrate Chemical compound O.[Na+].[Cl-] HPALAKNZSZLMCH-UHFFFAOYSA-M 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 238000007155 step growth polymerization reaction Methods 0.000 description 1
- LSNNMFCWUKXFEE-UHFFFAOYSA-L sulfite Chemical compound [O-]S([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-L 0.000 description 1
- 239000002600 sunflower oil Substances 0.000 description 1
- 229920005613 synthetic organic polymer Polymers 0.000 description 1
- 229920001059 synthetic polymer Polymers 0.000 description 1
- 235000010384 tocopherol Nutrition 0.000 description 1
- 229960001295 tocopherol Drugs 0.000 description 1
- 229930003799 tocopherol Natural products 0.000 description 1
- 239000011732 tocopherol Substances 0.000 description 1
- 231100000331 toxic Toxicity 0.000 description 1
- 230000002588 toxic effect Effects 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- 239000000080 wetting agent Substances 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
- 229920001285 xanthan gum Polymers 0.000 description 1
- GVJHHUAWPYXKBD-IEOSBIPESA-N α-tocopherol Chemical compound OC1=C(C)C(C)=C2O[C@@](CCC[C@H](C)CCC[C@H](C)CCCC(C)C)(C)CCC2=C1C GVJHHUAWPYXKBD-IEOSBIPESA-N 0.000 description 1
Classifications
-
- D—TEXTILES; PAPER
- D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
- D21H—PULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
- D21H23/00—Processes or apparatus for adding material to the pulp or to the paper
- D21H23/02—Processes or apparatus for adding material to the pulp or to the paper characterised by the manner in which substances are added
- D21H23/22—Addition to the formed paper
- D21H23/24—Addition to the formed paper during paper manufacture
- D21H23/26—Addition to the formed paper during paper manufacture by selecting point of addition or moisture content of the paper
-
- D—TEXTILES; PAPER
- D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
- D21H—PULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
- D21H17/00—Non-fibrous material added to the pulp, characterised by its constitution; Paper-impregnating material characterised by its constitution
- D21H17/71—Mixtures of material ; Pulp or paper comprising several different materials not incorporated by special processes
- D21H17/72—Mixtures of material ; Pulp or paper comprising several different materials not incorporated by special processes of organic material
-
- D—TEXTILES; PAPER
- D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
- D21H—PULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
- D21H21/00—Non-fibrous material added to the pulp, characterised by its function, form or properties; Paper-impregnating or coating material, characterised by its function, form or properties
- D21H21/14—Non-fibrous material added to the pulp, characterised by its function, form or properties; Paper-impregnating or coating material, characterised by its function, form or properties characterised by function or properties in or on the paper
- D21H21/22—Agents rendering paper porous, absorbent or bulky
- D21H21/24—Surfactants
-
- D—TEXTILES; PAPER
- D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
- D21H—PULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
- D21H23/00—Processes or apparatus for adding material to the pulp or to the paper
- D21H23/02—Processes or apparatus for adding material to the pulp or to the paper characterised by the manner in which substances are added
- D21H23/04—Addition to the pulp; After-treatment of added substances in the pulp
-
- D—TEXTILES; PAPER
- D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
- D21H—PULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
- D21H17/00—Non-fibrous material added to the pulp, characterised by its constitution; Paper-impregnating material characterised by its constitution
- D21H17/02—Material of vegetable origin
-
- D—TEXTILES; PAPER
- D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
- D21H—PULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
- D21H17/00—Non-fibrous material added to the pulp, characterised by its constitution; Paper-impregnating material characterised by its constitution
- D21H17/03—Non-macromolecular organic compounds
- D21H17/05—Non-macromolecular organic compounds containing elements other than carbon and hydrogen only
- D21H17/06—Alcohols; Phenols; Ethers; Aldehydes; Ketones; Acetals; Ketals
-
- D—TEXTILES; PAPER
- D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
- D21H—PULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
- D21H17/00—Non-fibrous material added to the pulp, characterised by its constitution; Paper-impregnating material characterised by its constitution
- D21H17/03—Non-macromolecular organic compounds
- D21H17/05—Non-macromolecular organic compounds containing elements other than carbon and hydrogen only
- D21H17/09—Sulfur-containing compounds
-
- D—TEXTILES; PAPER
- D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
- D21H—PULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
- D21H17/00—Non-fibrous material added to the pulp, characterised by its constitution; Paper-impregnating material characterised by its constitution
- D21H17/03—Non-macromolecular organic compounds
- D21H17/05—Non-macromolecular organic compounds containing elements other than carbon and hydrogen only
- D21H17/10—Phosphorus-containing compounds
-
- D—TEXTILES; PAPER
- D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
- D21H—PULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
- D21H17/00—Non-fibrous material added to the pulp, characterised by its constitution; Paper-impregnating material characterised by its constitution
- D21H17/03—Non-macromolecular organic compounds
- D21H17/05—Non-macromolecular organic compounds containing elements other than carbon and hydrogen only
- D21H17/14—Carboxylic acids; Derivatives thereof
-
- D—TEXTILES; PAPER
- D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
- D21H—PULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
- D21H17/00—Non-fibrous material added to the pulp, characterised by its constitution; Paper-impregnating material characterised by its constitution
- D21H17/60—Waxes
Landscapes
- Paper (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Abstract
The invention relates to a composition used for enhancing softness in paper products. The composition comprises (i) an oil, fat or wax (i) at least one non-ionic surfactant (iii) at least one anionic compound selected from anionic microparticles and anionic surfactants (iv) at least one polymer which is cationic, non-ionic or amphoteric wherein the non-ionic surfactant is added in an amount of from about 60 to about 1000 parts by weight per 100 parts by weight of the polymer. The invention also relates to a process for production of paper comprising adding said composition to a cellulosic suspension or to wet or dry paper web.
Description
COMPOSITION AND ITS USE IN PAPER MANUFACTURE The invention relates to a composition used to improve softness in paper products. The invention also relates to a papermaking process in which the composition is added to the cellulosic suspension or applied to a wet or dry paper web. The composition comprises an oil, wax or fat; at least one cationic, amphoteric or non-ionic polymer; and a compound selected from anionic surfactants and anionic microparticles; and one or more nonionic surfactants. Background
[0002] Wefts or sheets of paper, usually called thin paper or thin paper wefts, are commonly used in paper towels, napkins and thin facial paper and toilet paper. The important characteristics for these papers are softness, absorbency and strength. There is a work in progress to improve each of these characteristics without seriously affecting the others. Conventionally the thin pressed paper and methods for making such paper are well known in the art. Said paper is typically made by draining and forming a cellulosic suspension in a wire. The suspension
cellulosic is usually contained in the upper box before being deposited in a Fourdrinier wire to form a paper web. The paper web is then typically vacuum dehydrated by vacuum dewatering and further dried by pressing operations wherein the web is subjected to pressure developed by opposed mechanical members, for example cylindrical rollers or an extended grip press. The dehydrated web is then pressed and dried by a steam drum apparatus known in the art as a Yankee cylinder. Conventional fluff and methods for making such paper are well known in the art. Said paper is typically made by making a sheet of paper in a Fourdrinier wire and subsequently pressing and drying the paper sheet in bales or rolls. The dry paper is then defibrated using a hammer mill or a pin defibrator to form a fluff. The typical products made of fluff are diapers and feminine hygiene products. The fluff can also be used to produce paper products laid in the air. The softness is a tactile sensation perceived by the consumer that holds a particular product, rubbing it through the skin or rubbing it inside the hand. The
Softness of a sheet can be achieved by mechanical means.
For example, the sheet can be calendered to flatten the ridges formed when the sheet is pleated. The sheet can also be treated frictionally in order to eliminate any hardness. However, these approaches are often insufficient. One way to make paper softer is to add a softening compound to the cellulose suspension. The softening compound interferes with the natural fiber to fiber bond that occurs during sheet formation in papermaking processes. This reduction in bonding leads to a softer, or less rough, sheet of paper. WO 98/07927 describes the production of soft absorbent paper products using a softener. The softener comprises a quaternary ammonium surfactant, a nonionic surfactant as well as strength additives. The softening agent is added to the cellulosic suspension before the paper web is formed. A softening compound can also be applied to a dry or wet paper web, eg, by spraying. If the paper web is dry, the softener compound can also be printed on paper.
US 5,389,204 discloses a process for making soft thin paper with functional polysiloxane softener. The softener comprises a functional polysiloxane, an emulsifying surfactant and surfactants that are non-cationic. The softener is transferred to the dry paper web through a heater transfer surface. The softener is then pressed on the dry paper web. WO 97/30217 describes a composition used as a lotion to increase the softness of absorbent paper. The composition comprises an emollient which is preferably a fatty alcohol or a waxy ester. The composition also comprises a quaternary ammonium surfactant as well as one or more nonionic or amphoteric emulsifiers. Most softening compounds, whether added to the cellulose suspension or applied to the paper web, contain quaternary ammonium surfactants. Since producers and consumers experience increasing environmental importance, quaternary ammonium surfactants are not always accepted. Quaternary ammonium surfactants are generally toxic to aquatic organisms and are generally considered undesirable chemicals.
An object of the invention is to provide a composition for improving the softness of a paper product. A further object of the invention is to provide a composition substantially free of quaternary ammonium surfactants. Still another object of the invention is to provide a single composition suitable for addition to the cellulosic suspension and applied to a wet or dry paper web, instead of several different compositions as described in the above branch. Still a further object of the invention is to provide a composition which has a high tolerance towards the anionic transfer of preceding production steps. Conventional formulations in this manner can be neutralized at the wet end when small amounts of harmful substances are released from the preceding production steps. It is also an object of the invention to provide a composition which, when added to the cellulosic suspension, will impart low bursting resistance, high wetting rate as well as low defibration energy to the paper to be produced. It is also a further object of the invention
providing a composition which, when added to the cellulosic suspension, will impart a low knot content to the product. The Invention The invention relates to a composition used to improve softness in paper products, preferably products prepared from thin paper or fluff.
The composition can be applied in various stages in the papermaking process. The composition, for example, can be added at the wet end to the cellulosic suspension. A composition added to the cellulosic suspension to improve the softness of the product is called a detacher. The composition can also be applied to the paper web to improve the surface feel of the product, e.g., the softness. If the composition is applied to the wet paper web, the composition is called a softener. If the composition is applied to a dry paper web, the composition is called a lotion. The composition of the invention comprises (i) an oil, fat or wax (ii) at least one nonionic surfactant
(iii) at least one anionic compound selected from anionic icroparticles and
anionic surfactants (iv) at least one polymer that is cationic, nonionic or amphoteric wherein the nonionic surfactant is added in an amount of about 60 to about 1000 parts by weight per 100 parts by weight of the polymer. According to one embodiment, the composition is substantially free of quaternary ammonium surfactants. By "substantially free" is meant that less than 5% by weight of the composition is comprised of quaternary ammonium surfactants, such as less than 1% by weight, or less than 0.5% by weight. Any oil, grease or wax, which functions as an emollient, can be used in accordance with the invention. Suitable oils are refined and / or hydrogenated grade oils, such as vegetable oils, such as grapeseed oil, olive oil, coconut oil, rapeseed oil, sunflower oil, and palm oil, more preferably coconut oil . Other oils that can be used according to the invention are mineral oils and silicon oil. To retain the oil, grease or wax on a produced paper, a polymer that functions as an aid to
Retention is required. Polymers suitable for use as a retention agent or part of a retention system can be highly charged. According to one embodiment, the polymer is a cationic polymer. The polymers can be derived from natural or synthetic sources and can be linear, branched or crosslinked, e.g., in the form of microparticles. Preferably, the polymer is water soluble or dispersible in water. Examples of suitable natural cationic polymers include cationic polysaccharides, eg, starches, guar gums, cellulose derivatives, chitins, chitosans, glycans, galactans, glucans, xanthan gums, pectins, mannans, dextrins, preferably starches and guar gums. Suitable starches include potato, corn wheat, tapioca, rice, waxy maize, barley, etc. Cationic synthetic organic polymers such as cationic chain growth polymers can also be used, e.g., cationic vinyl addition polymer as acrylate, acrylamide, vinylamine, vinylamide and allylamine based polymers, for example homo- or copolymers based in diallyldialkyl ammonium halide, e.g. diallyldimethyl ammonium chloride, as well as
(meth) acrylamides and (meth) acrylates. Additional polymers
include cationic step growth polymers, e.g., cationic polyamido acids, polyethylene imines, polyamines, e.g., dimethylamine copolymers, epichlorohydrin; and polyurethanes. Additional examples of suitable cationic organic polymers include those described in WO 02/12626. According to one embodiment, the polymer is selected from the group consisting of polydiallydimethyl ammonium chloride, polyamines, cationic starch, amphoteric starch, and polyamidoamine-epichlorohydrin (PAAE), polyethylene imines or polyvinylamines. The term "step growth polymer", as used herein, refers to a polymer obtained by step growth polymerization, also being referred to as step reaction polymer and step reaction polymerization, respectively. The term "chain growth polymer", as used herein, refers to a polymer obtained by chain growth polymerization, also referred to as chain reaction polymer and chain reaction polymerization, respectively. The polymer according to the invention may have a molecular weight of about 10,000 to about
10000000, such as around 15,000 to about
5000000, or from around 40000 to around 1000000. According to one embodiment, an anionic microparticle is comprised in the composition. Examples of suitable anionic microparticles include anionic silica microparticles, such as anionic colloidal silica particles, and smectite clays, more preferably hydrophobically modified, anionic colloidal silica particles. The anionic microparticles preferably have a specific surface area of from about 40 to about 900, such as from about 150 to about 600, or from about 250 to about 400 m2 / g. The colloidal silica particles can be derived, e.g., from precipitated silica, micro silica (silica fume), fumed silica (fumed silica) or silica gels with sufficient purity, conventional sodium silicate and mixtures thereof. The colloidal silica particles according to the invention can be modified and can contain other elements such as amines, aluminum and / or boron, which may be present in the particles and / or the continuous phase. Boron-modified silica sols are described, e.g., in
US 2,630,410. The aluminum-modified silica particles appropriately have an A1203 content of from about 0.05 to about 3% by weight, such as from about 0.1 to about 2% by weight. The process for preparing an aluminum modified silica sol is further described e.g., in "The Chemistry of Silica," by Iler, K. Ralph, pages 407-409, John Wiley & Sons (1979) and US 5 368 833. The colloidal silica particles appropriately have an average particle diameter ranging from about 2 to about 150, such as from about 3 to about 50, or about 5. around 40 nm. Suitably, the colloidal silica particles have a specific surface area of from about 20 to about 1500, such as from about 50 to about 900, or from about 70 to about 600 m2 / g. The anionic surfactants which can be used according to the invention are generally anionic surfactants with hydrophobic "glues" having from about 6 to about 30 carbon atoms. Examples of preferred anionic surfactants are saponified fatty acids, alkyl (aryl) sulfonates, sulfate esters, phosphate esters, alkyl (aryl) phosphates,
alkyl (aryl) phosphonates, acid degrees, naphthalene sulfonate (ÑAS), polycondensates of formaldehyde, polystyrene sulfonates, ÑAS modified with hydrophobe. Saponified fatty acids are more preferred, alkyl (aryl) sulfonates, sulfate esters, phosphate esters, alkyl (aryl) phosphates, alkyl (aryl) phosphonates, and mixtures thereof. According to embodiment, the anionic compound is an anionic surfactant. The nonionic surfactants which can be used according to the invention generally include ethoxylated or propoxylated fatty acids or fatty alcohols. Ethoxylated fatty acids and fatty alcohols have been preferably ethoxylated with from about 1 to about 30 ethylene oxide (EO), or from about 4 to about 25 EO. The ethoxylated fatty acids and fatty alcohols can have from about 6 to about 30 carbon atoms, or from about 6 to about 22 carbon atoms. The propoxylated fatty acids and fatty alcohols may have been propoxylated with from about 1 to about 30 propylene oxide (PO), or from about 1 to about 8 PO. The propoxylated fatty acids and fatty alcohols preferably have
about 6 to about 30 carbon atoms, such as about 6 to about 22 carbon atoms.
It is also possible to use carbon dioxide instead of propylene oxide. The polymer is usually present in the composition in an amount of about 1 to about
50, such as from about 5 to about 40, or from about 10 to about 30% by weight based on the dry weight of the composition. The oil, fat or wax is usually present in the composition in an amount from about 1 to about 95, such as from about 30 to about 80, or from about 35 to about 75% by weight based on the dry weight of the composition. The anionic compound is suitably present in the composition in an amount from about 0.1 to about 10, such as from about 0.5 to about 4, or from about 0.6 to about 2% by weight based on the dry weight of the composition. According to one embodiment, the nonionic surfactant is present in an amount from about 70 to about 800, or from about 80 to
about 600, or from about 100 to about 500, or from about 150 to about 400 parts by weight per 100 parts by weight of the polymer. The composition can be prepared by first mixing the oil, fat or wax together with the anionic and nonionic surfactants to provide a mixture of emollient-surfactant. The emollient-surfactant mixture can be heated to about 25 to about 70 ° C. An aqueous solution containing the polymer is properly prepared in which solution the polymer content constitutes from about 0.1 to about 50, e.g., from about 0.5 to about 25% by weight. The aqueous solution can be heated to about 25 to about 70 ° C. The emollient-surfactant mixture can then be emulsified in the aqueous solution containing the polymer by a static mixer, an ultra-turrax high shear device or a homogenizer. The product emulsion can then be cooled to room temperature. Cooling, for example, can be done using a heat exchanger. According to one embodiment, the mixture of emollient and surfactant is emulsified to the
aqueous solution containing the polymer by means of a static mixer. The composition can be produced in advance and then delivered as a product to the paper mill. The composition can also be prepared on site in the paper mill of the different components. It is also possible to add additional components to the composition. To prevent deterioration of the composition, a preservative agent can be added. Various cosmetic additives may also be included, for example antioxidants, e.g., tocopherol, and aloe vera. The invention also relates to a process for the production of paper comprising adding the composition as described herein to a cellulosic suspension wherein the process further comprises draining the cellulosic suspension in a wire to form a paper web. According to one embodiment, the composition can be added in an amount from about 0.1 to about 15 kg / ton of dry cellulosic fibers. When the debonder is used to make the fluff, the composition is usually added to a cellulosic suspension in an amount of about 0.1 to about
15, such as from about 0.3 to about 10 kg / ton of dry cellulosic fibers. When the debonder is used to manufacture thin paper, the composition is usually added to a cellulosic suspension in an amount of about 0.1 to about
15, such as from about 0.5 to about 4 kg / ton of dry cellulosic fibers. When used as a debonder in this process, the composition, as already stated herein, is added to the cellulosic suspension before the paper web is formed. The use of detachers is very common when making borrilla and thin paper. The unloader will interfere with the natural fiber-to-fiber links so that the resistance is reduced. Reducing resistance, the softness of the fluff and the thin paper products is increased. According to one embodiment, the components of the composition can be added separately to the cellulosic suspension. Preferably, an emulsion of the oil, fat or wax and the anionic and nonionic surfactant can be added as a premix and a polymer, e.g., in an aqueous solution, can be added as a separate component to the cellulosic suspension. . In accordance with one modality, when
components are added separately, the amount of each component added to the cellulosic suspension corresponds to the amount of each component in the composition as described herein. In accordance with one embodiment, when making the fluff, the polymer can be added to a cellulosic suspension in an amount of about 0.01 to about 6 kg / ton of dry cellulosic fibers. In accordance with one embodiment, when making the fluff, the polymer can be added to a cellulosic suspension in an amount of about 0.025 to about 3.5 kg / ton of dry cellulosic fibers. In accordance with one embodiment, when making a fluff, the polymer can be added to a cellulosic suspension in an amount of about 0.05 to about 2.5 kg / ton of dry cellulosic fibers. According to one embodiment, when manufacturing brine, the oil, wax or grease can be added to a cellulosic suspension in an amount of about 0.001 to about 14 kg / ton of dry cellulosic fibers. According to one embodiment, when making a fluff, the oil, wax or grease can be added to a cellulosic suspension in an amount of about 0.03 to about 12 kg / ton of dry cellulosic fibers. From
In accordance with one embodiment, when making a fluff, the oil, wax or grease can be added to a cellulose suspension in an amount of about 0.035 to about 11 kg / ton of dry cellulosic fibers. According to one embodiment, when making a fluff, the anionic compound can be added to a cellulosic suspension in an amount of about 0.001 to about 1.5 kg / ton of dry cellulosic fibers. According to one embodiment, when making a fluff, the anionic compound can be added to a cellulosic suspension in an amount of about 0.003 to about 0.6 kg / ton of dry cellulosic fibers. According to one embodiment, when making a fluff, the anionic compound can be added to a cellulosic suspension in an amount of about 0.004 to about 0.3 kg / ton of dry cellulosic fibers. In accordance with one embodiment, when making a fluff, the nonionic surfactant is suitably added to the cellulosic suspension in an amount of from about 70 to about 800, such as from about 80 to about 600, or from about 100 to about 500, or from about 150 to about 400 parts by weight per 100 parts by weight of the polymer.
According to one embodiment, when making a fluff, the oil, wax or grease is added in an amount of about 0.001 to about 14 kg / ton of dry cellulosic fibers, the anionic surfactant compound is added in an amount of about 0.001 to about
1. 5 kg / ton of dry cellulosic fibers and the polymer is added in an amount of about 0.01 to about 6 kg / ton of dry cellulosic fibers. According to one embodiment, when thin paper is manufactured, the polymer can be added to a cellulosic suspension in an amount of about 0.01 to about 8 kg / ton of dry cellulosic fibers. According to one embodiment, when thin paper is made, the polymer can be added to a cellulosic suspension in an amount of about 0.03 to about 6 kg / ton of dry cellulosic fibers. According to one embodiment, when making thin paper, the polymer can be added to a cellulosic suspension in an amount of about 0.035 to about 5.5 kg / ton of dry cellulosic fibers. According to one embodiment, when thin paper is manufactured, the oil, wax or grease can be added to a cellulosic suspension in an amount of about 0.001 to
about 10 kg / ton of dry cellulosic fibers. In accordance with one modality, when thin paper is manufactured, the oil, wax or grease can be added to a cellulose suspension in an amount of about 0.03 to about 8 kg / ton of dry cellulosic fibers. According to one embodiment, when thin paper is manufactured, the oil, wax or grease can be added to a cellulosic suspension in an amount of about 0.035 to about 7.5 kg / ton of dry cellulosic fibers. According to one embodiment, when thin paper is made, the anionic compound can be added to a cellulosic suspension in an amount of about 0.001 to about 1 kg / ton of dry cellulosic fibers. According to one embodiment, when thin paper is manufactured, the anionic compound can be added to a cellulosic suspension in an amount of about 0.003 to about 0.4 kg / ton of dry cellulosic fibers. According to one embodiment, when making thin paper, the anionic compound can be added to a cellulosic suspension in an amount of about 0.004 to about 0.2 kg / ton of dry cellulosic fibers. According to one embodiment, when thin paper is manufactured, the nonionic surfactant is addedsuitably to the cellulosic suspension in an amount of from about 70 to about 800, such as about 80 to about 600, or from about 100 to about 500, or from about 150 to about 400 parts by weight per 100 parts by weight of the polymer. To evaluate the operation of the unloader, the bursting resistance, defibration energy and wetting regime can be measured. The low burst strength and low energy defibration shows that the fiber to fiber links are weak, which in turn facilitates the production of thin paper with improved smoothness. The wetting regime indicates that the finished product will have good absorption properties. Likewise, when using borrilla in airborne applications, it is important to minimize the number of knots. The knots can be described as bundles of fibers. A high number of knots can lead to low formation and running capacity in the process spread to the air. When the composition is applied to a wet or dry paper web, the surface touch can be improved. The superficial touch can be described as those superficial properties that are sensations
tactiles perceived by the consumer. Superficial touch can be evaluated by gene in panel tests. Examples of said properties are softness, slip and uniformity.
According to one embodiment, the composition is added to the sheet as a single addition. According to another embodiment, the polymer can be added to the cellulosic suspension before the formation of the weft, while the oil, wax or fat; the anionic compound; and the nonionic surfactant are added to the wet or dry paper web. The invention also relates to a process for the production of paper which comprises applying the composition as described herein to a wet paper web. When the composition is used as a softener in the papermaking process, the composition is usually sprayed onto the wet paper web after the press section but before the Yankee cylinder. By using the composition as a softener, it is possible to obtain a paper with high surface smoothness and minimum resistance reduction. According to one embodiment, when the composition is used as a softener in the manufacture of thin paper, the composition is usually added in a
amount from about 0.1 to about 10, preferably from about 0.3 to about 4 kg / ton of dry cellulosic fibers. The invention also relates to a process for the production of paper comprising applying the composition as described herein to a dry paper web. When the composition is used as a lotion in the above process, it is usually sprayed or printed onto the dry paper web. This is usually done in the conversion process in which the final thin paper product is formed. The lotion is properly present as drops on the wet surface of paper and is not bound to the fibers in the same way as a softener. The lotion modifies the surface properties of the thin paper, but the lotion is also added due to cosmetic reasons since the location can be released from the paper and transported to the consumer. According to one embodiment, the dry paper web has a dry content of at least about
50, such as at least about 65, or at least about 80% by weight. In accordance with one modality, when the
The composition is used as a lotion to make thin paper, the composition is usually added in the amount of from about 0.1 to about 70, such as around
5 to about 50 kg / ton of dry cellulose fibers. The cellulosic fibers used by the present invention will typically include fibers derived from wood pulp, which includes chemical pulp such as Kraft, sulphite and sulphate pulps, as well as mechanical pulps such as ground wood, thermomechanical pulp and thermomechanical pulp modified with chemicals. Recycled fibers can also be used. The recycled fibers can contain all the pulps mentioned above as well as fillings, printing inks, etc. Chemical pulps, however, are preferred since they impart a superior softness to thin paper sheets made therefrom. The use of recycled fibers to make frequent thin paper includes a process step known as de-inking to remove as much as possible the printing ink from the fiber suspension and most of the filler material to obtain an acceptable brightness and operating capacity. of recycled fiber suspension paper machine. The deinking process often includes the addition of anionic substances such as saponified fatty acids and glass of water to the
fiber suspension. These substances are sometimes taken to the paper machine and since these substances are anionic they can inactivate the cationic chemicals added to the material. These substances are called harmful anionic substances or "anionic garbage". According to one embodiment, additional components can be added to the cellulosic suspension used to make thin paper or fluff. These additives can be for example wet strength agents, dry strength agents, and wetting agents as well as other components usually used in the production process. According to one embodiment, an additional polymer that is either cationic, non-ionic or amphoteric can be added to the cellulosic suspension. Suitably the polymer is either a natural polymer, for example starch, or a synthetic polymer. According to one embodiment, an anionic polymer is added to the cellulosic suspension, these anionic polymers can include anionic per step growth polymers, chain growth polymers, polysaccharides, naturally occurring aromatic polymers and modifications thereof. The invention is further illustrated by the
following examples, but the invention is not intended to be limited thereto. EXAMPLE 1 Compositions according to the invention were prepared by first mixing coconut oil with a para-substituted alkylbenzylsulfonic acid (-C12) (anionic surfactant) and with an unsaturated fatty alcohol with
16 to 18 carbon atoms being ethoxylated with 5 EO (nonionic surfactant). The contents of the components were 50% by weight of oil, 25% by weight of anionic surfactant and 25% by weight of nonionic surfactant. The oil-surfactant mixture was then heated to 50 ° C. An aqueous polymer solution was prepared. The concentration of the polymer in the aqueous solution was between 1 to 4% by weight. The polymer concentration in the aqueous solution was between 1 to 4% by weight. The concentration of polymer for each composition is specified below. The aqueous polymer solution was heated separately at 50 ° C. The oil-surfactant mixture was then emulsified in the aqueous polymer solution in a high shear ultra-turrax. The composition was then cooled to room temperature in a water bath. The weight ratio of the oil-surfactant mixture to the solution
Aqueous was 15:85. The polymers and the concentrations thereof in the aqueous solutions used when preparing the C-1C6 compositions are listed below. Cl: 1% by weight of Poly-DADMAC (SNF No. FL45DL) C2: 3.4% by weight of Poly-DADMAC (SNF No. FL45DL) C3: 4% by weight of Poly-DADMDC (SNF No. FL45DL) C4: 1% by weight of Poly-DADMAC (SNF No. FL45C) C5: 4% by weight of Poly-DADMAC (SNF No. FL45C) C6: 1% by weight of Polyamine For comparison, developer compositions sold under the name Berocell® They were used. The contents of the two separator compositions Ref. 1 and Ref. 2 are shown below. Ref. 1: Berocell-589, benzyldimethylammonium chloride hydrogenated bait; fatty alcohol, with 5 unsaturated ethoxylated EO of C16-C18 Ref. 2: Berocell-509, dihydrogenated dimethylammonium chloride; fatty alcohol, ethoxylated with 6 unsaturated EO of C16-C20, C12-C18 fatty acid, propoxylated with 6PO The dried paper sheets were prepared by mixing 15 grams of chemical pine sulphate pulp with either water or
Contaminated white water up to 750 ml. The composition was added to the pulp suspension followed by 10 minutes of stirring. Next, a sheet was prepared in a conventional PFI sheet former (A4 sheets). The sheets were then pressed, dried and conditioned in accordance with the conventionalized method SCAN C26: 76. Example 2 Compositions C2 and C5 according to example 1 were compared with Ref. 1 (Berocell-589) as described in example 1. The compositions they were added to the cellulosic suspension in an amount of 3.0 kg / tonne based on dry cellulosic fibers. Dry paper sheets were then prepared as described in Example 1. The paper sheets were cut into strips and then defibrated with the help of a pin defibrator. The pin defibrator was connected to an energy meter that makes it possible to measure the energy consumption per kg of paper. The energy of defibration. The results are shown in table 1. Table 1. Defibration energy (kJ / kg)
Composition Running water White water C3 56 '74
C5 50 69 Ref. 1 61 88 A lower defibration energy will impart a higher degree of softness to the product. In Table 1, it is clearly shown that the compositions according to the invention, C3 and C5, impart lower defibration energy, which indicates improved softness compared to the composition according to the above branch, Ref. 1.
Example 3 Compositions Cl, C3, C4, C5 and C6 according to Example 1 were compared with Ref. 1 of Example 1. The compositions were added to the cellulosic suspension in an amount of 3.0 kg / ton based on dry cellulosic fibers. . Dry paper sheets were then prepared according to example 1. The moistening regime was measured on the dry paper sheets according to the conventionalized method SCAN-C33: 80. The results can be seen in table 2. Table 2. Composition Moisture Regimen (s / 3g pulp) Cl 3.8
C3 4.1 C4 4.0 C5 4.3 C6 3.9 Ref. 1 5.6 A low wetting rate is advantageous for both thin paper and fluff products. In table 2, it is clearly shown that the compositions according to the invention, Cl, C3, C4, C5 and C6, impart a wetting regime lower than a paper produced compared to the composition of the previous bouquet, Ref. 1. Example The composition C2 according to example 1 was compared with Ref. 2 of example 1. The amount of the composition added of the cellulose composition varied between
0. 5 and 4.0 kg / ton based on dry cellulosic fibers. Dry paper sheets were prepared from the cellulosic suspension as described in example 1. The burst strength was measured according to the conventional ISO 2758-2001 method. The results can be seen in table 3. Table 3 Burst Resistance (kPa% vs
Quantity added, reference Kg / ton of paper C2 Ref. 2 0.5 77 91 1.0 66 75 1.5 55 63 2.0 45 58 2.5 40 50 3.0 37 49 3.5 32 45 44..00 2200 43 The low resistance to burst will impart softness to the product. In Table 3, it is clearly shown that the composition C2, according to the invention, has a lower burst strength for various added amounts of the composition, compared to the composition according to the previous branch, Ref. 2. Example 5 The composition C2 according to example 1 was compared to Ref. 2 of example 1. The amount of composition added to the cellulosic suspension varied between 1 to 2 kg / ton based on dry cellulosic fibers. The knot content was measured using the conventional SCAN-CM 37 method. The results can be seen in the
Table 4. Table 4 Quantity added% of Knots Kg / ton dry paper C2 1 3.3 C2 2 1.1 Ref.l 1 4.2 Ref. 2 1.5 A high number of knots can lead to low running capacity and formation. Therefore, a low content of knots is advantageous. In table 4 it is clearly shown that the composition according to the invention,
C2, has a lower number of knots compared to Ref.2.
Example 6 An oil-surfactant mixture was prepared by first mixing coconut oil with an anionic surfactant, alkylbenzylsulfonic acid (-cl2), and two non-ionic surfactants (1) ethoxylated castor oil with
15 EO and (2) an unsaturated fatty alcohol of C16-C18 ethoxylated with 5 EO. The oil-surfactant mixture was then emulsified in water to form an oil emulsion. For
100 ml of water, 0.3 g of the oil-surfactant mixture was used. A solution of aqueous polymer containing
polyDADMAC was prepared with a polymer concentration of
0. 08% in weight. The dried paper sheets were prepared by mixing 15 grams of chemical pine sulphate pulp with water up to 750 ml. The oil emulsion was added to the pulp suspension.
The suspension was then stirred for 8 minutes. Then the polymer solution was added, after which the suspension was stirred for 2 minutes. After that, a sheet was prepared in a conventional PFI sheet former
(A4 sheets). The sheets were then pressed, dried and conditioned according to the conventionalized method
SCAN C26: 75. The amounts by weight of each component added in each test are given in Table 5. Table 5 Composition Oil of Agent Ten Agent Ten Agent Ten Poly- No. coconut surfactant active non-ionic nonionic non-ionic anionic (1) (2) 1 9.2 0.40 0.30 0.1 2.67
2 8.7 0.65 0.55 0.1 2.67
3 8.1 0.95 0.85 0.1 2.67
4 7.6 1.2 1.1 0.1 2.67
5 5.0 2.45 2.45 0.1 2.27
The ratio of nonionic surfactants to polymer was calculated as parts by weight of nonionic surfactants per 100 parts by weight of polymer. The energy of defibration was measured according to example 2. The added amount of the composition was 1 kg / ton and 3 kg / ton of dry cellulosic fibers. The results are given in Table 6. Table 6 Composition Tensioning parts - Desfine Energy. active nonionic / 100 brisation (kJulium / polymer parts kg) 1 kg / ton 3 kg / ton 28 132 124 45 135 115 3 67.5 103 67 4 86 98 64 5 216 93 62 A lower defibering energy will impart a higher degree of softness to the product. In Table 6 it can be clearly seen that the defibration energy decreases when the weight ratio of nonionic surfactants to polymer increases. Example 7
Two oil emulsions, El and E2, were prepared by mixing coconut oil with two nonionic surfactants (1) ethoxylated castor oil with 15 EO and (2) an unsaturated C16-C18 fatty alcohol ethoxylated with 5 EO. In the El emulsion, the weight ratio between coconut oil; nonionic surfactant (1) and nonionic surfactant (2) was 5: 2.5: 2.5, in emulsion E2, the corresponding ratio was 7: 1.5: 1.5. The oil emulsion was formed by emulsifying 15 g of the oil-surfactant mixture, by means of an ultra-turrax, in 85 g of a 0.353% by weight dispersion of a silica sol having a specific surface area of 525. m2 / g- An aqueous polymer solution containing polyDADMAC was also prepared at a concentration of 0.08% by weight. The dry paper sheets were prepared by mixing 15 grams of chemical pine sulphate pulp with water up to 750 ml. The oil emulsion was added to the pulp suspension after which it was stirred for 8 minutes. Then the polymer solution was added, after which the suspension was stirred for 2 minutes. Next, a sheet was prepared in a conventional PFI sheet former
(leaves A). The sheets were then pressed, dried and conditioned according to the conventionalized method
SCAN C26: 75. In test 3, a conventional unloader
Berocell 589, mentioned as Ref. 1 in Example 1, was used for comparison. When the sheet is made, the conventional debonder was added then the suspension was stirred during
10 minutes. The energy of defibration was measured according to example 2. The results are given in table 7. Table 7 Desfibration energy test (kJoule / kg) 1 The 64 2 E2 62 3 Ref.l The lower defibration energy will impart a high top of softness to the product. In table 7, it can be clearly seen that the compositions according to the invention El and E2, provide a lower defibration energy than the conventional debonder, Ref. 1. Example 8 The same mixture of oil-surfactant and polymer solution No. 5 in Table 5 was prepared in accordance with Example 6. In Test 1, the oil-surfactant mixture was emulsified in the solution of
polymer to form a single composition. Paper sheets were prepared by mixing 15 grams of chemical pine sulphate pulp with water up to 750 ml. The pulp suspension was then stirred for 10 minutes. In test 2, the polymer was added after 8 minutes of stirring. In tests 1 and 3, no additions were made to the pulp suspension. Thereafter, a sheet was prepared in a conventional PFI sheet former (A4 sheets). The sheets were then pressed at 4.85 Bar for 5 minutes resulting in a dry content of about 50% by weight. In test 1, the composition was sprayed towards the leaves, in the amount of 1 and 3 kg / ton of dry cellulosic fibers. In test 2, the oil emulsion containing the oil-surfactant mixture was sprayed onto the sheet so that the total addition, together with the polymer in the pulp suspension, was 1 and 3 kg / ton of cellulosic fibers dry. In test 3, a conventional Berocell unloader
589, referred to as Ref. 1 in Example 1, was used for comparison. The conventional debonder was also sprayed on the sheet in the amount of 3 1 and 3 kg / ton of dry cellulosic fibers. The leaves were then pressed at 4.85 Bar for 2
minutes, followed by drying in a drum at 80 ° C, for 2 h.
After drying the leaves were conditioned at 23 ° C and 50% relative humidity for at least 24 hours before testing. The defibration energy was then measured according to example 2, the knot content was measured according to the conventionalized method SCAN-CM 37 and the wetting regime was measured according to the conventionalized method SCAN-C33: 80. The results are given in Table 8. Table 8 Deficit Energy Test Humee regime- No. (b / kg /% 1 kg / ton 3 kg / ton lkg / ton 3kg / ton lkg / ton 3 kg / ton 1 97 78 4.68 3.00 4.2 4.4
2 93 83 3.66 1.67 4.4 4.7
3 122 84 4.00 2.67 5.0 5.2 The compositions in test 1 and test 2 show a clear improvement in energy of defibration, knot content and wetting regime compared to test 3 in which a conventional unloader was used. Example 9 A mixture of oil-surfactant was prepared
first mixing coconut oil with an anionic surfactant, alkylbenzylsulphonic acid (-C12), and two nonionic surfactants, (1) castor oil ethoxylated with
15 EO and (2) an alcohol grade unsaturated C16-C18 ethoxylated with 5 EO. The oil-surfactant mixture was then emulsified in water to form an oil emulsion. To 100 ml of water 0.3 g of the oil-surfactant mixture were used. An aqueous solution containing a cationic starch, amylofax PW, was prepared at a concentration of 0.08% by weight. The dried paper sheets were prepared by mixing 15 grams of chemical pine sulphate pulp with water up to 500 ml. The oil emulsion was added to the pulp suspension at time 0, followed by 10 minutes of stirring. The cationic starch was added after 8 minutes. After that, the sheet was prepared in a conventional PFI sheet former (A4 sheets). The sheets were then pressed, dried and conditioned in accordance with the conventionalized method SCAN C26: 76. The cationic starch was added in an amount of 2.5 kg / ton of dry cellulosic fibers. The addition of oil emulsion was varied between 0 and 3 kg / ton of dry cellulosic fibers. The
Defibration energy was measured according to example 2. The results are given in table 9.
Table 9 Desfibration energy (July / kg) Amount of oil emulsion added 0 kg / ton 1 kg / ton 2 kg / ton 3kg / ton 168 145 118 90 A lower defibration energy will impart a higher degree of softness to the product. In table 9 it can be clearly seen that the defibration energy decreases with an increased amount of oil emulsion.
Claims (1)
- CLAIMS 1. A composition comprising: (i) an oil, fat or wax (ii) at least one nonionic surfactant (iii) at least one anionic compound selected from anionic microparticles and anionic surfactants (iv) at least one polymer which is cationic, nonionic or amphoteric wherein the nonionic surfactant is added in an amount of from about 60 to about 1000 parts by weight per 100 parts by weight of the polymer. 2. A composition according to claim 1, wherein the composition is substantially free of quaternary ammonium surfactants. 3. A composition according to claim 1 or 2, wherein the polymer is a cationic polymer. 4. A composition according to claim 3, wherein the cationic polymer is a chain growth polymer. 5.- A composition in accordance with the claim 3, wherein the cationic polymer is a step growth polymer. 6. A composition according to any of the preceding claims, wherein the oil is a vegetable oil. 7. A composition according to any of the preceding claims, wherein the oil is a coconut oil. 8. A composition according to any of the preceding claims, wherein the nonionic surfactant is added in an amount of about 70 to about 800 parts by weight per 100 parts by weight of the polymer. 9. A composition according to any of the preceding claims, wherein the nonionic surfactant is added in an amount of about 80 to about 1000 parts by weight per 100 parts by weight of the polymer. 10. A composition according to any of the preceding claims, wherein the nonionic surfactant is added in an amount of from about 100 to about 800 parts by weight per 100 parts by weight of the polymer. 11. - A composition according to any of the preceding claims, wherein the nonionic surfactant is an ethoxylated or propoxylated fatty alcohol or fatty alcohol. 12. A composition according to any of the preceding claims, wherein the anionic surfactant is selected from the group consisting of saponified fatty acids, alkyl (aryl) sulfonates, sulfate esters, phosphate esters, alkyl (aryl) phosphates , alkyl (aryl) phosphonates and mixtures thereof. 13. A process for producing paper that comprises adding the composition according to any of claims 1 to 12 to a cellulosic suspension, wherein the process further comprises draining the cellulosic suspension in a wire to form a paper web. 14. A process for the production of paper according to claim 13, wherein the composition is added in an amount of about 0.1 to about 15 kg / ton of dry cellulose fibers. 15. A process for the production of paper, comprising adding (i) an oil, fat or wax (ii) at least one nonionic surfactant (iii) at least one anionic compound selected from anionic microparticles and anionic surfactants (iv) at least one polymer that is cationic, non-cationic or amphoteric, to a cellulosic suspension, wherein the process further comprises draining the cellulosic suspension in a wire to form a paper web, wherein the nonionic surfactant is added in an amount of from about 60 to about 1000 parts by weight per 100 parts by weight of the polymer. 16. A process for the production of paper according to claim 15, wherein the oil, wax or fat is added in an amount of about 0.01 to about 14 kg / ton of dry cellulosic fibers, the compound anionic is added in an amount of about 0. 001 to about 1.5 kg / ton of dry cellulosic fibers and the polymer is added in an amount of about 0. 01 to around 6 kg / ton of dry cellulose fibers. 17. A process for the production of paper that comprises applying the composition in accordance with any of claims 1 to 12 to a wet paper web. 18. A process according to claim 17, wherein the composition is applied in an amount of about .1 to about 10 kg / ton of dry cellulosic fibers. 19. A process for the production of paper that comprises applying the composition according to any of claims 1 to 12 to a dry paper web. 20. A process according to claim 19, wherein the composition is applied in an amount of from about 0.1 to about 70 kg / ton of dry cellulosic fibers. 21. A process according to any of claims 13 to 20, wherein the nonionic surfactant is added in an amount of from about 80 to about 1000 parts by weight per 100 parts by weight of the polymer. 22. A process according to any of claims 13 to 20, wherein the nonionic surfactant is added in an amount of about 100 to about 1000 parts by weight per 100 parts by weight of the polymer.
Applications Claiming Priority (2)
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|---|---|---|---|
| EP04107059 | 2004-12-30 | ||
| PCT/SE2005/001927 WO2006071175A2 (en) | 2004-12-30 | 2005-12-15 | Composition and its use in papermaking |
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| MX2007006733A true MX2007006733A (en) | 2007-07-25 |
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| BR (1) | BRPI0519782A2 (en) |
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| WO (1) | WO2006071175A2 (en) |
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|---|---|---|---|---|
| PL2462277T3 (en) | 2009-08-05 | 2015-04-30 | Int Paper Co | Process for applying composition containing a cationic trivalent metal and debonder and fluff pulp sheet made from same |
| MY162376A (en) | 2009-08-05 | 2017-06-15 | Shell Int Research | Method for monitoring a well |
| CN104947509B (en) | 2009-08-05 | 2017-11-03 | 国际纸业公司 | Dry fluff pulp sheet additive |
| BR112013010261A2 (en) * | 2010-10-29 | 2016-09-13 | Buckman Lab Int Inc | method for preparing paper or cardboard, papermaking system, paper product and paper product |
| US8518214B2 (en) * | 2011-07-18 | 2013-08-27 | Nalco Company | Debonder and softener compositions |
| CN110306375A (en) * | 2019-07-10 | 2019-10-08 | 姜秀财 | One kind pasting Mare Nectairs mulberry paper manufacturing method |
| FR3113069B1 (en) * | 2020-07-30 | 2022-10-14 | Snf Sa | PAPER AND CARDBOARD MANUFACTURING PROCESS |
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| CH660015A5 (en) * | 1982-02-01 | 1987-03-13 | Sandoz Ag | PREPARATIONS CONTAINING POLYMER AND SURFACTANTS, THEIR PRODUCTION AND USE. |
| JPS5916510A (en) * | 1982-02-01 | 1984-01-27 | サンド・アクチエンゲゼルシヤフト | Hydrophilic cation polymer |
| DE3327600A1 (en) * | 1983-07-30 | 1985-02-14 | Sandoz-Patent-GmbH, 7850 Lörrach | PREPARATIONS CONTAINING COPOLYMERS AND TENSIDES, THEIR PRODUCTION AND USE |
| SU1397587A1 (en) * | 1986-12-25 | 1988-05-23 | Центральный научно-исследовательский институт бумаги | Method of producing fluidized fibrous cellulose-containing material for sanitary paper articles |
| SE500387C2 (en) | 1989-11-09 | 1994-06-13 | Eka Nobel Ab | Silica sols, process for making silica sols and using the soles in paper making |
| GR920100221A (en) * | 1991-07-19 | 1993-05-24 | Johnson & Johnson Inc | Flexible absorbent sheet. |
| JPH05310540A (en) * | 1992-05-13 | 1993-11-22 | Kao Corp | Liquid detergent composition |
| US5389204A (en) * | 1994-03-10 | 1995-02-14 | The Procter & Gamble Company | Process for applying a thin film containing low levels of a functional-polysiloxane and a mineral oil to tissue paper |
| US5698076A (en) * | 1996-08-21 | 1997-12-16 | The Procter & Gamble Company | Tissue paper containing a vegetable oil based quaternary ammonium compound |
| FR2745016B1 (en) * | 1996-02-19 | 1998-04-17 | James River | COMPOSITION FOR A SOFTENING LOTION, USE OF THE LOTION FOR THE TREATMENT OF AN ABSORBENT PAPER PRODUCT AND ABSORBENT PAPER PRODUCT THUS TREATED |
| SE9601135D0 (en) * | 1996-03-25 | 1996-03-25 | Eka Nobel Ab | Absorbent cellulosic material and production thereof |
| JPH10265352A (en) * | 1997-03-25 | 1998-10-06 | Shiseido Co Ltd | Oil-in-alcohol type hair set composition |
| US6288019B1 (en) * | 1998-11-12 | 2001-09-11 | Colgate-Palmolive Co. | Microemulsion liquid cleaning composition containing a short chain amphiphile |
| CO5170451A1 (en) * | 1999-04-23 | 2002-06-27 | Kimberly Clark Co | WET CLEANING PANOS THAT HAVE HEALTH BENEFITS FOR THE SKIN |
| CN1331971C (en) * | 2000-06-09 | 2007-08-15 | 赵志刚 | Leather dry cleaning finishing cream |
| US6815403B1 (en) * | 2002-07-18 | 2004-11-09 | Kenneth T. Laney | Toilet drain cleaning composition |
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- 2005-12-15 JP JP2007549315A patent/JP4672736B2/en not_active Expired - Fee Related
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- 2005-12-15 MX MX2007006733A patent/MX2007006733A/en active IP Right Grant
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Also Published As
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| CA2594011A1 (en) | 2006-07-06 |
| NZ555799A (en) | 2011-01-28 |
| BRPI0519782A2 (en) | 2009-03-17 |
| AU2005322662B2 (en) | 2009-02-12 |
| KR100919463B1 (en) | 2009-09-28 |
| JP4672736B2 (en) | 2011-04-20 |
| CN101094956A (en) | 2007-12-26 |
| ZA200704974B (en) | 2008-09-25 |
| AU2005322662A1 (en) | 2006-07-06 |
| CN101094956B (en) | 2011-05-25 |
| KR20070101297A (en) | 2007-10-16 |
| RU2347030C1 (en) | 2009-02-20 |
| JP2008527072A (en) | 2008-07-24 |
| EP1831462A2 (en) | 2007-09-12 |
| WO2006071175A3 (en) | 2007-01-11 |
| CA2594011C (en) | 2011-08-09 |
| WO2006071175A2 (en) | 2006-07-06 |
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